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home > Book 3A: 2026 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor Responsibilities > Book 3A: 2026 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor Responsibilities
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Book 3A: 2026 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor ResponsibilitiesDescription Contents Cover This spiral bound, 5" x 7. 5" book is a compilation of the FDA Information Sheets, selected government regulations, and other helpful documents that address the protection of human subjects in research. It includes such topics as: Informed Consent The Common Rule (45 CFR Part 46) Protection of Human Subjects Reviewing and Reporting Unanticipated Problems The HIPAA Privacy Rule in Research Recruiting Study Subjects Who Uses
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Book 3A:  2026 Selected Regulations and Guidance on Protection of Human Subjects:  Clinical Investigator, IRB & Sponsor Responsibilities

Book 3A: 2026 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor Responsibilities

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